Product Details

SNP ID: rs16841987
Assay Type: Functionally tested
NCBI dbSNP Submissions: 31
Location: Chr.1:159295476 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CATTTATTTATTATCAATGAAAAAC[A/G]TACAAATTTTCTAATTAAAAAACTT
Phenotype: MIM: 147140
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: FCER1A PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002001.3		Intron			NP_001992.1